HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methyl-2-butene → 1-Benzyl-2-isopropyl-6-methoxy-1H-indole-3-carboxylic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methyl-2-butene | HCID 10553 | — |
| Reactant | Monobasic potassium phosphate | HCID 516951 | — |
| Reactant | Sodium Chlorite | HCID 23668197 | — |
| Reactant | 1-Benzyl-2-isopropyl-6-methoxy-1H-indole-3-carbaldehyde | HCID 59762394 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 1-Benzyl-2-isopropyl-6-methoxy-1H-indole-3-carboxylic Acid | HCID 59762354 | — |
Reaction Steps
To a solution of 1-benzyl-2-isopropyl-6-methoxy-1H-indole-3-carbaldehyde (Compound 5, 608 mg, 1.98 mmol) in t-BuOH (15 ml), CH3CN (15 ml), and 2-methyl-2-butene (10 ml) was added a solution of KH2PO4 (5.4 g, 39.6 mmol) and NaClO2 (80%, 4.5 g, 39.6 mmol) in H2O (50 ml). The mixture was stirred at room temperature and additional 2-methyl-2-butene, KH2PO4, and NaClO2 were added at the above ratio every 16-24 h until the starting material was consumed. The reaction mixture was extracted with EtOAc (×3) and the combined organic layer was washed with brine, dried over Na2SO4, and concentrated in vacuo. The residue was purified by chromatography on silica gel (0→25% EtOAc-hexanes) to yield the title compound as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08524917B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-df34ff595be44ca7a2a241a02c99ab6e |
| Source note | uspto-grants-2013_09 |